sildenafil
Generic: sildenafil
Labeler: preferred pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
sildenafil
Generic Name
sildenafil
Labeler
preferred pharmaceuticals, inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
sildenafil citrate 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68788-7879
Product ID
68788-7879_be069c7b-77d7-4eee-b686-969fd72b8d84
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202659
Listing Expiration
2026-12-31
Marketing Start
2021-03-08
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687887879
Hyphenated Format
68788-7879
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
sildenafil (source: ndc)
Generic Name
sildenafil (source: ndc)
Application Number
ANDA202659 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 10 TABLET, FILM COATED in 1 BOTTLE (68788-7879-1)
- 7 TABLET, FILM COATED in 1 BOTTLE (68788-7879-7)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "be069c7b-77d7-4eee-b686-969fd72b8d84", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["314229"], "spl_set_id": ["174ef537-e3e6-42bd-a478-47b930ddc761"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (68788-7879-1)", "package_ndc": "68788-7879-1", "marketing_start_date": "20210308"}, {"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE (68788-7879-7)", "package_ndc": "68788-7879-7", "marketing_start_date": "20210308"}], "brand_name": "Sildenafil", "product_id": "68788-7879_be069c7b-77d7-4eee-b686-969fd72b8d84", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "68788-7879", "generic_name": "Sildenafil", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "100 mg/1"}], "application_number": "ANDA202659", "marketing_category": "ANDA", "marketing_start_date": "20210308", "listing_expiration_date": "20261231"}